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Celecoxib add on therapy in drug naive depressed women

A Randomized, Double-blind, Placebo-controlled trial of Celecoxib augmentation of Sertraline in treatment of Drug-Naïve depressed women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201009043106N3
Enrollment
40
Registered
2010-11-14
Start date
2008-07-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

major depressive disorder. Depressive episode

Interventions

Intervention 1: Celecoxib group: 25-100mg/day Sertraline plus 100mg Celecoxib twice daily for eight weeks. Intervention 2: Control group: 25-100mg/day Sertraline plus 100mg placebo twice daily for eig
Treatment - Drugs
Placebo
Celecoxib group: 25-100mg/day Sertraline plus 100mg Celecoxib twice daily for eight weeks.
Control group: 25-100mg/day Sertraline plus 100mg placebo twice daily for eight weeks.

Sponsors

Pharmaceutical Sciences Branch of Islamic Azad university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. women experiencing first episode of depression according to DSM-IV-TR and the Hamilton rating scale (17 items) score was ranged from 18 to 36. 2. None of them had previously received antidepressant treatment. Exclusion criteria: 1. History of taking antidepressant medications. 2. Other psychiatric disorders. 3. Significant suicidal ideation. 4. lactation and pregnancy. 5. Liver and kidney dysfunction and cardiovascular disorders. 6. Drug abuse.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression severity. Timepoint: baseline, week 4 and week 8. Method of measurement: Hamilton Depression rating scale -17 items.;Anxiety severity. Timepoint: baseline, week 4 and week 8. Method of measurement: Hamilton Anxiety rating scale.

Secondary

MeasureTime frame
General health level. Timepoint: baseline, week 4 and week 8. Method of measurement: General health questionnair-28.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026